Canonical Allele Identifier: CA384973659
Gene: KRT75 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52827645C>G (hg19) chr12:g.52433861C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433861C>G , CM000674.2:g.52433861C>G GRCh38
NC_000012.11:g.52827645C>G , CM000674.1:g.52827645C>G GRCh37
NC_000012.10:g.51113912C>G NCBI36
NG_008403.1:g.5466G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.444G>C MANE Select ENSP00000252245.5:p.Glu148Asp
ENST00000252245.5:c.444G>C ENSP00000252245.5:p.Glu148Asp
NM_004693.2:c.444G>C NP_004684.2:p.Glu148Asp
NM_004693.3:c.444G>C MANE Select NP_004684.2:p.Glu148Asp
Search 100 bp 5'
Search 100 bp 3'